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rs28416813

From SNPedia

Orientationplus
Stabilizedplus
Make rs28416813(C;C)
Make rs28416813(C;G)
Make rs28416813(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position39245004
GeneIFNL3
is asnp
is mentioned by
dbSNPrs28416813
ebirs28416813
HLIrs28416813
Exacrs28416813
Varsomers28416813
Maprs28416813
PheGenIrs28416813
hapmaprs28416813
1000 genomesrs28416813
hgdprs28416813
ensemblrs28416813
gopubmedrs28416813
geneviewrs28416813
scholarrs28416813
googlers28416813
pharmgkbrs28416813
gwascentralrs28416813
openSNPrs28416813
23andMers28416813
23andMe allrs28416813
SNP Nexus

SNPshotrs28416813
SNPdbers28416813
MSV3drs28416813
GWAS Ctlgrs28416813
GMAF0.3301
Max Magnitude

[PMID 19749757] Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C




GET Evidence
rs28416813
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.380718
summary



[PMID 24116050OA-icon.png] A Single Nucleotide Polymorphism Associated with Hepatitis C Virus Infections Located in the Distal Region of the IL28B Promoter Influences NF-κB-Mediated Gene Transcription